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The Brainstem Pathologies of Parkinson's Disease and Dementia with Lewy Bodies

机译:路易体的帕金森氏病和痴呆症的脑干病理

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Parkinson's disease (PD) and dementia with Lewy bodies (DLB) are among the human synucleinopathies, which show alpha-synuclein immunoreactive neuronal and/or glial aggregations and progressive neuronal loss in selected brain regions (eg, substantia nigra, ventral tegmental area, pedunculopontine nucleus). Despite several studies about brainstem pathologies in PD and DLB, there is currently no detailed information available regarding the presence of alpha-synuclein immunoreactive inclusions (i) in the cranial nerve, precerebellar, vestibular and oculomotor brainstem nuclei and (ii) in brainstem fiber tracts and oligodendroctyes. Therefore, we analyzed the inclusion pathologies in the brainstem nuclei (Lewy bodies, LB; Lewy neurites, LN; coiled bodies, CB) and fiber tracts (LN, CB) of PD and DLB patients. As reported in previous studies, LB and LN were most prevalent in the substantia nigra, ventral tegmental area, pedunculopontine and raphe nuclei, periaqueductal gray, locus coeruleus, parabrachial nuclei, reticular formation, prepositus hypoglossal, dorsal motor vagal and solitary nuclei. Additionally we were able to demonstrate LB and LN in all cranial nerve nuclei, premotor oculomotor, precerebellar and vestibular brainstem nuclei, as well as LN in all brainstem fiber tracts. CB were present in nearly all brainstem nuclei and brainstem fiber tracts containing LB and/or LN. These findings can contribute to a large variety of less well-explained PD and DLB symptoms (eg, gait and postural instability, impaired balance and postural reflexes, falls, ingestive and oculomotor dysfunctions) and point to the occurrence of disturbances of intra-axonal transport processes and transneuronal spread of the underlying pathological processes of PD and DLB along anatomical pathways.
机译:帕金森氏病(PD)和路易体痴呆(DLB)是人类的突触核病,在特定的大脑区域(例如黑质,腹侧被盖区,足小脑桥骨)显示α-突触核蛋白免疫反应性神经元和/或神经胶质聚集以及进行性神经元丧失。核)。尽管对PD和DLB的脑干病理进行了多项研究,但目前尚无关于α-突触核蛋白免疫反应性内含物(i)在颅神经,小脑前庭,前庭和动眼动脑干核中和(ii)在脑干纤维束中存在的详细信息。和oligodendroctyes。因此,我们分析了PD和DLB患者脑干核(路易体,LB;路易神经突,LN;螺旋体,CB)和纤维束(LN,CB)中的包涵病理。如先前的研究报道,LB和LN最常见于黑质,腹侧被盖区,足小脑桥骨和沟核,水管周围灰质,蓝斑,臂臂旁核,网状结构,垂体舌下舌下,背运动迷走神经和孤立核。此外,我们能够在所有颅神经核,运动前动眼动,小脑前庭和前庭脑干核以及所有脑干纤维道中的LN中证实LB和LN。在几乎所有含有LB和/或LN的脑干核和脑干纤维束中均存在CB。这些发现可能会导致大量无法充分解释的PD和DLB症状(例如步态和姿势不稳,平衡和姿势反射受损,跌倒,摄食和动眼功能障碍),并提示发生轴突内运输障碍PD和DLB沿解剖途径的潜在病理过程的过程和跨神经元扩散。

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